Additional Effects of Joint Mobilization in Addition to Rocabado Exercises on Alleviating Trismus Following Third Molar Extraction

July 30, 2024 updated by: Foundation University Islamabad
Without appropriate early intervention, prolonged trismus can lead to lasting complications like reduced jaw mobility or temporomandibular joint disorders.Therefore joint mobilization will impact on trismus, that will offer valuable insights into how these interventions will affect inflammation, muscle function and overall healing process within TMJ besides rocabado exercises that involves a series of movements and stretches targeting the muscles and joints involved in chewing,swallowing and speaking and minimizing muscle tension and opening the mouth, preventing further deterioration of jaw function and improving overall quality of life of individuals. If found effective, this will be added to the literature for the treatment of trismus after third molar extraction.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

54

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • Foundation University College of Physical Therapy

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Referral or consultation from a dentist to confirm the diagnosis of trismus.
  • Age 18-45 years
  • Both genders (Male and Female)
  • Maximal interincisal opening ≤ 35mm (Restricted jaw motion).
  • Unilateral/Bilateral impacted lower third molars.
  • 3 days Post mandibular Third molar extraction

Exclusion Criteria:

  • Local Infection or bleeding post third molar extraction.
  • Patients with Acute pericoronitis
  • Patient undergoing chemotherapy and radiotherapy.
  • Type I diabetes, renal failure and chronic liver disease were excluded as immunocompromised state.
  • Pregnant or lactating women.
  • Cyst or tumor associated with impacted tooth

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Maitland joint mobilization + Rocabdo exercises

Therapeutic ultrasound: pulse mode - 1:4, frequency 3 MHz, intensity- 0.8 watt/cm2 for about 3-4 Minutes.

Mobilizations will be performed in Grade 1 initially and then progressed to Grade 2 and 3.

Techniques used are anterior, lateral and inferior glides Frequency: 3-4 times in 1 week . 4 sessions in total.

Therapeutic ultrasound: pulse mode - 1:4, frequency 3 MHz, intensity- 0.8 watt/cm2 for about 3-4 minutes.
6 Rocabado exercises 6 Reps each.

Mobilizations will be performed in Grade 1 initially and then progressed to Grade 2 and 3.

Techniques used are anterior, lateral and inferior glides

Experimental: Rocabado exercises

Participants of this Group will receive the conventional physical therapy along with 6 Rocabado exercises.6 reps each Therapeutic ultrasound: pulse mode - 1:4, frequency 3 MHz, intensity- 0.8 watt/cm2 for about 3-4 Minutes.

Frequency: 3-4 times in 1 week . 4 sessions in total.

Therapeutic ultrasound: pulse mode - 1:4, frequency 3 MHz, intensity- 0.8 watt/cm2 for about 3-4 minutes.
6 Rocabado exercises 6 Reps each.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain intensity
Time Frame: 1 week
pain will be measured using Numeric pain rating scale
1 week
Range of motion
Time Frame: 1 week
A Vernier caliper will be used to measure maximal incisal opening (MIO) ≤ 35 mm (ROM)
1 week
Functional Performance
Time Frame: 1 week
Gothenburg Trismus Questionnaire will be used for assessing functional performance or trismus-related quality of life.
1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 10, 2024

Primary Completion (Estimated)

December 10, 2024

Study Completion (Estimated)

December 30, 2024

Study Registration Dates

First Submitted

July 30, 2024

First Submitted That Met QC Criteria

July 30, 2024

First Posted (Actual)

August 2, 2024

Study Record Updates

Last Update Posted (Actual)

August 2, 2024

Last Update Submitted That Met QC Criteria

July 30, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • FUI/CTR/2024/18

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Trismus

Clinical Trials on Electrotherapy

Subscribe